Polo-like kinase1, a new target for antisense tumor therapy

被引:33
作者
Elez, R
Piiper, A
Giannini, CD
Brendel, M
Zeuzem, S
机构
[1] JW Goethe Univ, Dept Med 2, D-60590 Frankfurt, Germany
[2] JW Goethe Univ, Inst Mikrobiol, D-60590 Frankfurt, Germany
关键词
D O I
10.1006/bbrc.2000.2291
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Polo-like kinase 1 (Plk1) is a highly conserved mitotic serine/threonine kinase which is commonly overexpressed in cancer cell lines. Plk1 positively regulates mitotic progression by activating the CDC25C-CDK1 amplification loop and by regulating late mitotic events, primarily the ubiquitin-dependent proteolysis. In the present study, an antisense strategy against Plk1 mRNA was developed to specifically inhibit cell proliferation of cancer cells in cell culture and in the nude-mouse tumor model. Among 41 phosphorothioate antisense oligodeoxynucleotides tested, the 20-mer JWG2000 strongly inhibited expression of Plk1 in cultured A549 cells, leading to loss of cell viability, and exhibited anti-tumor activity in nude mice A549 xenograft. JWG2000 did not inhibit growth and viability of primary human mesangial cells and human amnion fibroblasts. (C) 2000 Academic Press.
引用
收藏
页码:352 / 356
页数:5
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